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Syncope Steen Juul-Möller , MD, PhD, FESC Dpt. of Cardiology Skane University Hospital, Malmö, Sweden ”ECG Monitoring”

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Syncope  

Steen Juul-Möller, MD, PhD, FESC Dpt. of Cardiology Skane University Hospital, Malmö, Sweden

”ECG Monitoring”

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…there  are  many  kinds…  

…some  TLOC`s  have  a    permanent  impact…  

…others  are  of  a  more  paroxysmal  nature…  

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…  and  some  are  mostly  to  show  the  world  …  

..that  I  am  a  misunderstood  Darling!  

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The  first  quesEon  is  

Why?  Vessel  tone?  

Heart?  Europace,  2002;4:351-­‐356  

56%  

14%  

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Heart! Structural    

or  

Arrhythmia  

Europace,  2002;4:351-­‐356  

3%  

11%  

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Arrhythmia?    

Only  one  requirement!    You  need  an    

ECG-­‐strip  from  the  event!  As  always,  a  few  excepEons:  •   Slow  AF  or  AFl  •   AV  block  2-­‐3  •   Extreme  sinus  bradycardia  •   Trifascicular  block  •   WPW/Brugada  Syndrome,  etc.  

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Our  methods:  

•  12-­‐lead  ECG  

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Our  methods:  

•  12-­‐lead  ECG  •  1/2/7  days  Ambulatory  ECG  (Holter)  

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The  original  Holter  biotelemetry  Apparatus.  From  1947,    Weighing  38  kg  

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The  original  Holter  biotelemetry  Apparatus  In  1947,    weighing  85  lb  (38  kg)  

118  g  splashproof  

The  original  Holter  biotelemetry  Apparatus.  From  1947,    Weighing  38  kg  

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Our  methods:  

•  12-­‐lead  ECG  •  1/2/7  days  Ambulatory  ECG  (Holter)  

•  External  Loop  Recorder  

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Our  methods:  

•  12-­‐lead  ECG  •  1/2/7  days  Ambulatory  ECG  (Holter)  

•  External  Loop  Recorder  •  Ambulatory  short-­‐strip  ECG  

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Our  methods:  

•  12-­‐lead  ECG  •  1/2/7  days  Ambulatory  ECG  (Holter)  

•  External  Loop  Recorder  •  Ambulatory  short-­‐strip  ECG  

•  Implantable  Cardiac  Monitor  

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Our  methods:  

•  12-­‐lead  ECG  •  1/2/7  days  Ambulatory  ECG  (Holter)  

•  External  Loop  Recorder  •  Ambulatory  short-­‐strip  ECG  

•  Implantable  Cardiac  Monitor  

•  Pacemaker/ICD  

•  In-­‐Hospital  ECG  monitoring  

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We  want  to  get  the  culprit-­‐ECG  as  easy  and  efficient  as  we  can!  

At  the  ECG-­‐lab  in  Malmö  we  perform  3400  Holters/year.  We  perform  all  kind  of    

ECG-­‐invesEgaEons.  

This  report  demonstrates  the    

diagnosEc  efficacy  2008-­‐2009.  

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 StaEsEcs  2008-­‐2009  n=6250  

24  hours  Holter   62%  

48  hours   23%  

7  days     15%  

External  Loop    Recorder   60/year  

ICM        18/year  

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The  DiagnosEc  QuesEons    > one question in 20%

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Syncope:  Types  

22 Europace,  2002;4:351-­‐356  

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Syncope:  Types  

23 Europace,  2002;4:351-­‐356  

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Syncope:  Types  

24 Europace,  2002;4:351-­‐356  

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Did  we  answer  the  clinical  quesEon?    (All  invesEgaEons  from  2009;  n=3200)  

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Next  step:  External  Loop-­‐recorder!  2008-­‐9  years  invesEgaEons;  n=120  

No  symptoms:  No  ECG        Mean  dura4on:  4.2  weeks  (2-­‐14  wks)  

ECG  during  symptoms  

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Next  step:  External  Loop-­‐recorder!  2008-­‐9  years  invesEgaEons;  n=120  

No  symptoms:  No  ECG        Mean  dura4on:  4.2  weeks  (2-­‐14  wks)  

ECG  during  symptoms  

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Next  step:  External  Loop-­‐recorder!  2008-­‐9  years  invesEgaEons;  n=120  

No  symptoms:  No  ECG        Mean  dura4on:  4.2  weeks  (2-­‐14  wks)  

ECG  during  symptoms  

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18  of  the  120  paEents  w/  External  Loop-­‐Recorder  had  syncope  during  

the  test.  

Bradycardia:  2  paEents  (11%)  

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18  of  the  120  paEents  w/  External  Loop-­‐Recorder  had  syncope  during  

the  test.  

Normal  sinus  rhythm:  72%  

Single  extra  beats:  17%  

Bradycardia:  2  paEents  (11%)  

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…  the  last  resort    …    Implantable  Cardiac  Monitor  

6250  Holters    

Arrhythmia  (63%)  

Syncope  (n=25%)  

Inconclusive  in  35%  

Ischemia  (25%)  

Other  (6%)  

External Loop Recorder (n=120) Inconclusive in 29%

ICM (n=36) 5% of all Syncope patients

For  the  years  2008-­‐9:  

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The  diagnosEc  efficacy  of  ICM  has  been  evaluated  in  the    

PICTURE-­‐study  

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Primary  Objec4ve  •  To  evaluate  the  Eme  to  diagnosis  in  relaEon  to  the  Eming  of  the  Reveal  implant  during  the  diagnosEc  workup.  

Secondary  Objec4ves  •  Determine  diagnosEc  yield  •  Describe  the  standard  care  pathway    •  Evaluate  the  total  burden  of  diagnosEc  tests  (early  use  vs.  late  use)  •  Determine  the  raEo  between  diagnosis  “cardiac  related”  and  “non-­‐cardiac  

related”.    •  RelaEonship  between  results  of  diagnosEc  tests  and  Reveal  diagnosis.  •  Differences  in  recurrence  rate  syncope  vs.  presyncope  •  Determine  the  relaEonship  between  #  preceding  syncopal  events  vs.  Eme  to  

diagnosis.  

PICTURE  –  Primary  and  secondary  objecEves  

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PICTURE  study  plan  

•  PICTURE  was  a  prospecEve,  mulE-­‐centre,  observaEonal  post-­‐markeEng  study  conducted  from  November  2006  unEl  October  2009  

•  88  parEcipaEng  sites  in  11  countries  (Austria,  the  Czech  Republic,  Denmark,  Finland,  France,  Germany,  Israel,  The  Netherlands,  the  Slovak  Republic,  Sweden  and  Switzerland).  A  total  of  72  sites  contributed  to  paEent  enrolment.  

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PICTURE  study  plan  •  PaEents  were  eligible  if  they  had  recurrent  unexplained  syncope  or  pre-­‐syncope.    

•  PaEents  were  followed  up  unEl  the  first  recurrence  of  a  syncopal  event  leading  to  a  diagnosis  or  for  at  least  1  year.  

•  650  paEents  enrolled  (2006-­‐2008)  

•  570  paEents  followed-­‐up  

•  Average  Follow-­‐Up  Eme:  10±6  months  

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Time  to  recurrence  of  syncope,  ater  Reveal  implant  

•  During  follow-­‐up  a  total  of  218  paEents  (38%  of  the  populaEon)  experienced  an  episode  of  syncope,  149  with  prodromal  symptoms  

•  The  percentages  of  paEents  that  had  a  recurrence  of  syncope  were  19%,  26%  and  36%  ater  3,  6  and  12  months  respecEvely  (black  line)  

•  10%  of  paEents  with  an  episode  during  follow-­‐up  had  associated  severe  trauma.  

Recurrence  of  Syncope,  first  year:  36%  

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DiagnosEc  yield  of  Reveal  •  Time  to  a  syncopal  event  where  

Reveal  played  a  role  in  the  diagnosis  showed  the  recurrence  of  diagnosis  within  180  days  as  20%,  within  365  days  as  30%  and  within  462  days  as  38%  (grey  line)  

•  The  esEmated  rate  of  syncope  ater  30  days  of  follow-­‐up  was  10%  and  the  esEmated  rate  of  diagnosis  where  Reveal  played  a  role  at  this  Eme  of  follow-­‐up  was  9%  

ICM  played  a  diagnosEc  role,  first  year:  30%  

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Conclusion:  •  11%  of  paEents  with  Syncope  have  Arrhythmogenic  Syncope.  

•  The  majority  (67%)  can  be  evaluated  using  Holter.  DiagnosEc  in  65%.  

•  External  Event  Recorder  is  needed  by  25%.  DiagnosEc  in  11%  of  those  with  Syncope.  

•  ICM  is  indicated  in  5%  of  the  Syncope  paEents  in  whom  a  diagnosis  can  be  obtained  in    

  30%  within  1  year  .  

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Arrhythmic  Syncope  EvaluaEon:  

11%  

89%  

100%  

67%  

25%  

5%  

Arrh.  Syncope  

Other  Syncope  

1-­‐7  d  Holter  

External  Event  Recorder  

Implantable  Cardiac  Monitor  

1-­‐7  d  

4  weeks  

>  1  year  

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Conclusion:  

We  get  them  all…  

        eventually!!  

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Thank You For your attention!

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It is over!!